Spondyloarthritis & psoriatic arthritis
Clinical and pharmacological outcomes after switching from intravenous to subcutaneous infliximab in chronic inflammatory rheumatic diseases
Authors' conclusion
These findings support the effectiveness of SC IFX in maintaining disease control in CIR, with a favorable safety profile and significant economic benefits.
Study context
- Population
- Adults with controlled chronic inflammatory rheumatic diseases (16 axSpA, 5 PsA, 1 unclassified CIR) on intravenous (IV) infliximab, single centre73 eligible
- Participants
- 22 vs 13
- Exposure
- Subcutaneous (SC) infliximab after switch from IV infliximab
- Enrolledn = 22
- Routine caren = 13
- Outcome
- Retention on SC IFX (enrolled patients)
- Follow-up
- 6 and 12 months
Methodological detailssingle-center, non-medical switch, Outcomes collected at 3, 6, and 12months; Infliximab (IFX) concentrations and anti-IFX antibodies at baseline, 6months, and 12months
- Single-center
- Non-medical switch
- Outcomes collected at 3, 6, and 12months; IFX concentrations and anti-IFX antibodies at baseline, 6months, and 12months
Main finding
As reported in the abstract
Patients remaining on SC IFX at 6 and 12 months
19 of 22
86%
Observational data: associations, not effects.
Further findings
Mean serum IFX level before scheduled IV infusion (baseline)
- Mean serum IFX level
- 11±7μg/mL
Mean serum IFX level after switch to SC · 6 months
- Mean serum IFX level
- 30±17.6μg/mL
Mean serum IFX level after switch to SC · 12 months
- Mean serum IFX level
- 25.6±13.1μg/mL
Anti-drug antibodies
- No anti-drug antibodies detected
Patient satisfaction (out of 10)
- Mean satisfaction score
- 9.7±0.37
Retention on SC IFX, patients switched in routine care · one year
- Remained on SC IFX
- 8/13
Annual mean treatment cost per patient, SC IFX vs IV IFX
- SC IFX €4,627±23 vs IV IFX €7,456±1,331
- P < 0.001
- Significantly lower with SC IFX
Safety
Mild adverse events
- Patients reporting mild AEs
- 6
- Pruritus
- 1
- Injection pain
- 2
- Injection-site reactions
- 4
- Resolved in all but one patient by study end
Original publication
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